Add to ORKGThe core structure of the natural sesquiterpene lactones furanoheliangolides, an 11-oxabicyclo[6.2.1]undecane system, was synthesized through a pathway involving two Diels-Alder reactions. (c) 2007 Elsevier Ltd. All rights reserved
The research described herein focuses on the development of novel methods and synthetic sequences to...
Since the initial report by Diels and Alder in 1928, the [4+2] cycloaddition remains one of the most...
Diels-Alder reaction of 1,3,3-trimethyl-2-vinylcyclohexene I with conjugated ketones 2 - 7 in the pr...
The core structure of the natural sesquiterpene lactones furanoheliangolides, an 11-oxabicyclo[6.2.1...
Furanoeliangolidos são produtos naturais biologicamente ativos que contêm um esqueleto 11-oxabiciclo...
Furanoeliangolidos são produtos naturais biologicamente ativos que contêm um esqueleto 11-oxabiciclo...
Nosso grupo de pesquisa já vem há alguns anos estudando métodos para a síntese do núcleo estrutural ...
AbstractA bicyclo[6.2.1]undecane model compound of the core structure of the biologically active fur...
O objetivo deste trabalho foi iniciar o estudo de uma nova metodologia sintética para a obtenção do ...
O objetivo deste trabalho foi desenvolver métodos para sintetizar o esqueleto carbônico básico de fu...
This thesis has got two parts within the common theme of Diels-Alder reactions. One part starts with...
The total synthesis of complex natural products remains one of the enduring challenges in organic ch...
It was the purpose of this thesis work to develop new cyclization sequences to be used toward the sy...
A novel method for annulating furans to ketones, involving treatment of the dichlorocarbene adduct o...
A new strategy for the synthesis of sesquiterpenoids of the furanoeremophilane family was developed ...
The research described herein focuses on the development of novel methods and synthetic sequences to...
Since the initial report by Diels and Alder in 1928, the [4+2] cycloaddition remains one of the most...
Diels-Alder reaction of 1,3,3-trimethyl-2-vinylcyclohexene I with conjugated ketones 2 - 7 in the pr...
The core structure of the natural sesquiterpene lactones furanoheliangolides, an 11-oxabicyclo[6.2.1...
Furanoeliangolidos são produtos naturais biologicamente ativos que contêm um esqueleto 11-oxabiciclo...
Furanoeliangolidos são produtos naturais biologicamente ativos que contêm um esqueleto 11-oxabiciclo...
Nosso grupo de pesquisa já vem há alguns anos estudando métodos para a síntese do núcleo estrutural ...
AbstractA bicyclo[6.2.1]undecane model compound of the core structure of the biologically active fur...
O objetivo deste trabalho foi iniciar o estudo de uma nova metodologia sintética para a obtenção do ...
O objetivo deste trabalho foi desenvolver métodos para sintetizar o esqueleto carbônico básico de fu...
This thesis has got two parts within the common theme of Diels-Alder reactions. One part starts with...
The total synthesis of complex natural products remains one of the enduring challenges in organic ch...
It was the purpose of this thesis work to develop new cyclization sequences to be used toward the sy...
A novel method for annulating furans to ketones, involving treatment of the dichlorocarbene adduct o...
A new strategy for the synthesis of sesquiterpenoids of the furanoeremophilane family was developed ...
The research described herein focuses on the development of novel methods and synthetic sequences to...
Since the initial report by Diels and Alder in 1928, the [4+2] cycloaddition remains one of the most...
Diels-Alder reaction of 1,3,3-trimethyl-2-vinylcyclohexene I with conjugated ketones 2 - 7 in the pr...